Expiry Date: 28-02-2020
Category Regulatory Affairs
Salary: On Application
Job Type: Full Time
Regulatory Affairs CMC Biologicals Role *** Covering the full project lifecycle Manager *** Based in Brussels
We have a new role based in Brussels, Belgium for a Global pharmaceutical company who are now extensively expanding their Global RA CMC team.
My client is a highly rated and extremely successful Bio-Pharmaceutical company with a Global reach. They are seeking Regulatory Affairs CMC professionals who have experience in Biologicals (mAbs, Vaccines, Proteins) for roles that will grow to cover the full project lifecycle, from early phase development to supporting initial MAA’s and global market expansion projects (to include, Japan, China, LatAm and Asia-Pac), whilst maximizing the business benefits balanced with regulatory compliance.
The roles are broad based and varied role and will include further training and development in:
You will need to have at least 18 months of regulatory affairs CMC experience with a commercial or academic background in Biotechnology. My client is offering a strong salary at the upper end of the pay scale with a number of strong benefits/initiatives around full re-location, private healthcare, sign-on allowance, and strong overall benefits package.
To apply for this role, please press the red “Apply for position” button, or contact Theo Moore on +44 (0)207 801 3384 or Oli Dimitrov on +44 (0)207 801 3388 in full confidence to receive more details on this role or to hear about other available opportunities in Regulatory Affairs.
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